(Q33147836)
Statements
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Homozygotous mutation of the SCN5A gene responsible for congenital long QT syndrome with 2/1 atrioventricular block (English)
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Lupoglazoff JM
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Denjoy I
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Cheav T
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Berthet M
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Extramiana F
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Cauchemez B
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Villain E
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Leenhardt A
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Guicheney P
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1 May 2002
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95
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440-446
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Identifiers
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